20741502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971918-T-A

20741530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971855-T-C

20741539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971846-C-T

20741693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971715-C-T

20741809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971626-T-C

20741923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971526-C-T

20741925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971524-T-C

20741981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971474-G-A

20742378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971089-A-T

20742416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137971046-T-C

20744237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969574-T-C

20744261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969547-C-G

20744261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969547-C-T

http://identifiers.org/hco/1/GRCh38#20744329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137969483-C-A

20744380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969436-T-C

20744382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969434-G-T

http://identifiers.org/hco/1/GRCh38#20744455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137969379-C-A

20744455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969379-C-T

20744486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969348-A-G

20744683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969161-T-A

20744702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137969143-T-C

20744854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137968992-T-C

20744930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137968916-C-G

20745019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137968827-T-C

20745052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137968794-G-A

20745052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137968794-G-T

http://identifiers.org/hco/1/GRCh38#20745153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137968695-A-C

http://identifiers.org/hco/1/GRCh38#20745218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137968633-A-C

20745402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137968353-T-C

20745532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137968056-C-T

20745606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137967980-T-C

20745612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137967974-T-C

20745612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137967974-T-G

20745669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967917-A-G

20745699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967897-A-G

20745713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967883-T-C

20745733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967866-C-T

20745877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967752-C-T

http://identifiers.org/hco/1/GRCh38#20745938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137967697-A-C

20745938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137967697-A-G

20747577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137966924-C-G

http://identifiers.org/hco/1/GRCh38#20747712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137966795-C-A

20747712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966795-C-T

http://identifiers.org/hco/1/GRCh38#20747732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137966775-C-A

20747736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966771-A-G

20748145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966561-C-T

20748463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966309-T-A

20748463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966309-T-C

20748655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966099-G-A

20748655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966099-G-C

20748655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966099-G-T

20748682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966073-C-T

20748697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966058-G-A

20748765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137966014-A-T

http://identifiers.org/hco/1/GRCh38#20748907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137965256-C-A

20748918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137965245-A-G

20748940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137965214-T-C

20748965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137965192-G-A

20749007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137965150-G-C

20749701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137964638-A-G

20749701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137964638-A-T

20749739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137964600-G-C

20749856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137964483-C-T

http://identifiers.org/hco/1/GRCh38#20750056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137964284-C-A

20750056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964284-C-G

20750056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964284-C-T

20750091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964249-C-T

http://identifiers.org/hco/1/GRCh38#20750124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137964215-A-C

20750124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964215-A-T

http://identifiers.org/hco/1/GRCh38#20750151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137964187-A-C

20750154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964184-G-A

20750154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964184-G-C

20750154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964184-G-T

20750233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137964050-G-A

20750290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137963997-T-C

20757038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961736-G-T

http://identifiers.org/hco/1/GRCh38#20757260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137961548-C-A

20757260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137961548-C-T

20757280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961536-A-G

20757280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961536-A-T

20757355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137961462-T-C

20765108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958078-G-A

20765120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958066-G-A

20765120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958066-G-C

20765122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137958064-T-C

http://identifiers.org/hco/1/GRCh38#20765174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137958016-C-A

http://identifiers.org/hco/1/GRCh38#20765225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137957954-C-A

20765555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957650-A-T

http://identifiers.org/hco/1/GRCh38#20765574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137957632-A-C

20765574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957632-A-G

http://identifiers.org/hco/1/GRCh38#20765595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137957601-A-C

20767398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957229-T-G

20767432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957207-A-T

http://identifiers.org/hco/1/GRCh38#20767494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137957139-C-A

20767494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957139-C-G

20767494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957139-C-T

20767528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957117-A-G

20767528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957117-A-T

20767529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137957116-T-C

20767694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956958-T-C

http://identifiers.org/hco/1/GRCh38#20767780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137956876-A-C

20767780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956876-A-G

20769770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956804-C-T

20770784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956216-T-C

20770806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956194-A-G

20770806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956194-A-T

20770836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956167-A-T

http://identifiers.org/hco/1/GRCh38#20770893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137956129-C-A

20770893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956129-C-T

20770912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956114-C-T

20770921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956105-G-A

20770921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137956105-G-T

http://identifiers.org/hco/1/GRCh38#20770988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137956038-C-A

20771085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137955944-T-G

20771129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137955893-T-C

http://identifiers.org/hco/1/GRCh38#20771211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137955823-C-A

http://identifiers.org/hco/1/GRCh38#20773332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137953475-A-C

20773332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953475-A-G

20773332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953475-A-T

http://identifiers.org/hco/1/GRCh38#20773335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137953472-A-C

20773335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953472-A-T

20773363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953444-T-C

20773363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953444-T-G

20773411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137953397-A-G

20773506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137953302-G-A

20773506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137953302-G-C

20773572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137953236-T-C

20773644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137953166-A-G

20773663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137953147-T-C

20773663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137953147-T-G

http://identifiers.org/hco/1/GRCh38#20773838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137952503-C-A

20773838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137952503-C-G

http://identifiers.org/hco/1/GRCh38#20776207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137951332-A-C

http://identifiers.org/hco/1/GRCh38#20776215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137951324-A-C

20776220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951319-T-C

http://identifiers.org/hco/1/GRCh38#20776256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137951285-C-A

20776256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951285-C-G

20776256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951285-C-T

http://identifiers.org/hco/1/GRCh38#20776299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137951243-C-A

20776299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951243-C-T

20776301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951241-T-A

20776301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951241-T-C

http://identifiers.org/hco/1/GRCh38#20776362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137951179-A-C

20776376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951165-G-A

20776376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951165-G-C

20776389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951159-T-C

20776405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951150-C-T

20776469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951085-T-A

20776514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951040-G-C

20776514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951040-G-T

20776526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137951028-T-A

20776614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137950941-A-G

20776614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137950941-A-T

20776622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 137950933-T-A

20776622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137950933-T-C

20776624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137950931-T-C

20776705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137950844-T-C

http://identifiers.org/hco/1/GRCh38#20776803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137950745-C-A

http://identifiers.org/hco/1/GRCh38#20776883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137950649-A-C

20776883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137950649-A-G

20779211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137950011-A-G

20779426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949807-G-A

20779666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949605-T-C

20779699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949576-A-G

20779736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949544-T-A

20779736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949544-T-C

20779944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949358-A-G

20779944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949358-A-T

20779988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949317-G-A

20779988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949317-G-T

20779997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949306-G-A

20779997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949306-G-T

20780045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949259-T-A

20780045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949259-T-G

20780063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949241-G-A

20780063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137949241-G-T

20780373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137949004-T-G

20780393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 137948984-G-C

20780393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 137948984-G-T

20780427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948950-G-A

20780427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948950-G-C

20780427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948950-G-T

20780442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948935-T-C

20780442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948935-T-G

20780461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948916-G-A

20780461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948916-G-C

20780461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948916-G-T

20780481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948896-A-G

20780494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948883-A-G

20780513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137948862-A-T

20780542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 137948833-T-A

20780542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 137948833-T-C

20780550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948825-A-G

http://identifiers.org/hco/1/GRCh38#20780581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137948794-C-A

http://identifiers.org/hco/1/GRCh38#20780586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137948789-C-A

20780586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948789-C-G

20780586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948789-C-T

20780957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948447-T-C

20780971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948430-C-T

20781031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137948374-C-T

20786326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137944898-G-C

20786535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944698-C-T

20786676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944567-G-A

20786676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944567-G-T

20786820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944424-G-A

20786820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944424-G-T

20786965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137944275-G-A

20786965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137944275-G-T

20786966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137944274-G-A

20787050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944193-G-A

20787128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944117-G-A

20787128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944117-G-C

20787128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137944117-G-T

http://identifiers.org/hco/1/GRCh38#20787291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137943960-C-A

20787291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24973
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137943960-C-T